Although texts recommend the generation of rich data from interviews, no empirical evidence base exists for achieving this. This study aimed to operationalise richness and to assess which components of the interview (for example, topic, interviewee, question) were predictive. A total of 400 interview questions and their corresponding responses were selected from 10 qualitative studies in the area of health identified from university colleagues and the UK Data Archive database. The analysis used the text analysis program, Linguistic Inquiry and Word Count, and additional rating scales. Richness was operationalised along five dimensions. 'Length of response' was predicted by a personal, less specific or positive topic, not being a layperson, later questions, open or double questions; 'personal richness' was predicted by being a healthy participant and questions about the past and future; 'analytical responses' were predicted by a personal or less specific topic, not being a layperson, later questions, questions relating to insight and causation; 'action responses' were predicted by a less specific topic, not being a layperson, being healthy, later and open questions. The model for 'descriptive richness' was not significant. Overall, open questions, located later on and framed in the present or past tense, tended to be most predictive of richness. This could inform improvements in interview technique.
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http://dx.doi.org/10.1111/j.1467-9566.2010.01272.x | DOI Listing |
J Fr Ophtalmol
December 2024
Kayseri City Hospital, Department of Ophthalmology, Kayseri, Turkey.
Ther Innov Regul Sci
January 2025
GSK HQ, 79 New Oxford Street, London, WC1A 1DG, UK.
The European Union Clinical Trials Regulation (EU CTR) provides new regulatory requirements for the preparation and submission of clinical trial documents. The United Kingdom Drug Information Association Medical Writing (UK DIA MW) Committee, with members from across the pharmaceutical industry, have reviewed the EU CTR and in this report, provide expert guidance on writing documents for submission in the EU CTR Clinical Trials Information System (CTIS) portal. Medical writers should be aware that the Investigator's Brochure containing the Reference Safety Information (RSI) must align with the annual safety report, and the RSI format must comply closely with the EU CTR.
View Article and Find Full Text PDFJ Med Internet Res
October 2024
Center for Biomedical and Health Research in Data Sciences, Miner School of Computer and Information Sciences, University of Massachusetts Lowell, Lowell, MA, United States.
Cureus
September 2024
Department of Emergency Medicine, Amrita Institute of Medical Sciences, Kochi, IND.
Nature
October 2024
Sloan School of Management, Massachusetts Institute of Technology, Cambridge, MA, USA.
In response to intense pressure, technology companies have enacted policies to combat misinformation. The enforcement of these policies has, however, led to technology companies being regularly accused of political bias. We argue that differential sharing of misinformation by people identifying with different political groups could lead to political asymmetries in enforcement, even by unbiased policies.
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